FdaApplication
ANDA 072637
Identifiers
- fda_app_no: ANDA072637
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | ANDA |
| approval_date | 1989-12-05 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | EQ 2MG BASE | TABLET;ORAL |
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | EQ 4MG BASE | TABLET;ORAL |
2 products